덴마크 비타민 C 가격 및 무역 — 마켓 오버뷰 2026

상위 제품

단일 비타민 원료

하위 제품

아스코르브산, 아스코르빌 팔미테이트, 칼슘 아스코르베이트, 소듐 아스코르베이트

최종 업데이트

2026-10-08

서치 및 소싱 팀을 위한 핵심 요약

이 페이지 데이터셋의 최신 기준 연도는 2024입니다.
페이지 데이터 최종 업데이트일: 2026-10-08.

소싱 진단

덴마크산 비타민 C, 우리도 들여올 수 있을까요?

필요한 스펙과 물량만 알려주세요. 실제로 소싱이 되는지, 어떤 원산지와 공급사가 맞는지 짚어드려요.

무료 진단, 계정 없이 이용 가능합니다.

덴마크의 비타민 C 수입 바이어 인텔리전스 및 가격 시그널: 바이어, 수요, 거래 파트너

수출업체와 수입업체는 Supply Chain Intelligence 기업 프로필 및 분석으로 덴마크의 비타민 C 구매 수요, 파트너 밀도, 다운스트림 채널을 분석할 수 있습니다.

덴마크 내 비타민 C의 연간 수입 금액, 물량 및 수요 규모 (HS 코드 -)

덴마크의 비타민 C 수입 물량/금액 3년치를 추적해 수요 성장과 시장 모멘텀을 평가하세요.

연도	물량	금액
2024	980,676	3,269,687 USD
2023	839,659	3,292,508 USD
2022	914,114	5,145,168 USD

덴마크에 비타민 C를 공급하는 주요 원산지 공급국 (HS 코드 -) 2024

2024년 기준, 덴마크로 비타민 C를 공급하는 상위 원산 공급국 5개 전반의 수입 물량과 금액을 비교하세요.

순위	국가	물량	금액
1	독일	616,602	1,770,276.422 USD
2	중국	251,922	617,230.609 USD
3	네덜란드	65,324	383,776.504 USD
4	이탈리아	13,400	82,272.322 USD
5	폴란드	2,794	78,861.043 USD

수출 진단

우리 비타민 C, 이 덴마크 바이어들에게 팔 수 있을까요?

만드시는 제품만 알려주시면 됩니다. 지금 수출할 준비가 됐는지, 어느 시장이 맞는지 봐드려요.

무료 진단, 계정 없이 이용 가능합니다.

가격 데이터

덴마크 비타민 C 가격, 어디까지 필요하세요?

전체 가격 히스토리와 경쟁사 벤치마크를 열어드립니다. 어떤 숫자가 필요하신지만 말씀해 주시면 함께 살펴봐 드려요.

Classification

Product TypeProcessed Food

Product FormShelf-stable (dietary supplement: tablet/capsule/effervescent)

Industry PositionConsumer Packaged Dietary Supplement

Market

Vitamin C supplements in Denmark are a year-round, shelf-stable consumer health category sold primarily through regulated food-supplement channels under EU food law and Danish enforcement. Market access is shaped by compliance with EU rules on labeling and permitted nutrition/health claims, plus Danish authority guidance and controls. Denmark functions mainly as an import-supplied consumer market for both finished supplements and vitamin C inputs used by brand owners and contract manufacturers. The most trade-critical risk is regulatory non-compliance (borderline medicinal classification, unauthorized claims, or labeling errors), which can trigger withdrawal or rejection.

Market RoleImport-dependent consumer market (EU single-market distribution with reliance on imported finished supplements and imported vitamin C inputs)

Domestic RoleConsumer market for dietary supplements; local brand ownership and retail programs exist alongside imported brands.

Market Growth

SeasonalityYear-round availability and demand; not driven by agricultural harvest seasonality.

Specification

Primary VarietyL-ascorbic acid (Vitamin C)

Secondary Variety

Sodium ascorbate
Calcium ascorbate
Ascorbyl palmitate (in some formulations)

Physical Attributes

Tablet/capsule integrity and uniformity (appearance, breakage resistance)
Effervescent tablet performance (dissolution behavior and packaging moisture protection)
Packaging integrity (child-resistant closures where used, tamper evidence, blister seal quality)

Compositional Metrics

Declared vitamin C content per daily portion and compliance with tolerances
Stability over shelf life under labeled storage conditions
Impurity and contaminant controls aligned with applicable food-safety requirements

Grades

Food-grade vitamin C inputs with documented specifications (identity/purity) for supplement manufacturing

Packaging

HDPE/PET bottles with desiccant for tablets/capsules
Blister packs (unit-dose) for tablets
Tubes or sachets for effervescent tablets
Danish-language labeling compliant with EU requirements

Supply Chain

Value Chain

Imported vitamin C ingredient and/or finished products → (optional) EU/Denmark contract manufacturing and packaging → Danish-language labeling and responsible operator assignment → wholesale/distributor → retail (pharmacy/drugstore/e-commerce)

Temperature

Ambient distribution typical; storage conditions should follow labeled instructions to preserve declared potency.

Shelf Life

Moisture-control packaging is particularly important for effervescent formats and some tablet formulations.

Freight IntensityLow

Transport ModeMultimodal

Risks

Regulatory Classification HighVitamin C products can be rejected, withdrawn, or reclassified if the presentation (claims), dosage form, or dosage positioning causes them to be treated as a medicinal product or if claims are not compliant with EU rules; this is a primary deal-breaker risk for Denmark market access.Pre-check borderline status and claims strategy against Danish authority guidance; use only authorised EU health claims, avoid medicinal positioning, and keep a documented substantiation file and compliant Danish labeling.

Regulatory Compliance MediumNon-compliant labeling (mandatory statements, language, or nutrition/ingredient presentation) can trigger enforcement action, product relabeling, or delisting from pharmacy/drugstore programs.Run a Denmark-specific label compliance review against EU 1169/2011 and food-supplement rules; validate artwork control and versioning with importer-of-record.

Food Safety MediumImpurities, contamination, or mislabeling of nutrient content (under- or over-delivery vs. declared amount) can trigger recalls and authority action under official controls frameworks.Use qualified suppliers with robust incoming QC (identity/purity), perform finished-product verification testing, and maintain lot-based traceability and recall drills.

Documentation Gap MediumGaps in traceability, supplier declarations, or claim substantiation documentation can delay listings with regulated channels and increase exposure during official controls.Maintain a controlled technical file (specs, COAs, traceability, allergen/excipient declarations, claims substantiation) and ensure rapid retrieval for audits.

Sustainability

Packaging waste and recyclability expectations for consumer supplement formats (bottles, blisters, effervescent tubes)
Supplier environmental management screening for chemically manufactured inputs (energy and chemical safety management)

Labor & Social

Supply-chain due diligence expectations for upstream chemical manufacturing and contract manufacturing (worker safety, ethical sourcing audits)
Retailer and distributor compliance programs may require documented social/compliance policies from private-label and branded suppliers

Standards

HACCP-based food safety management (aligned with EU hygiene requirements)
ISO 22000 or FSSC 22000 (often requested in private supply contracts)
GMP-aligned manufacturing controls for dietary supplements (private/contractual requirement in many supply chains)

FAQ

Which core EU rules most directly govern vitamin C supplements sold in Denmark?Vitamin C supplements placed on the Danish market are generally governed by the EU Food Supplements framework (including Directive 2002/46/EC), EU food information/labeling rules (Regulation (EU) No 1169/2011), and EU nutrition and health claims rules (Regulation (EC) No 1924/2006, using only authorised claims from the EU register), alongside Danish enforcement by Fødevarestyrelsen.

What is the biggest compliance risk that can block a vitamin C supplement from being sold in Denmark?The biggest blocker is regulatory non-compliance—especially using non-authorised health claims or presenting the product in a way that triggers medicinal classification/borderline concerns—because this can lead to withdrawal, relabeling requirements, or refusal to list the product in key channels.

What traceability level is expected for vitamin C supplements in Denmark?EU General Food Law traceability expectations apply, meaning the operator should be able to identify immediate suppliers and immediate customers (one step back/one step forward) and run effective lot-based recall procedures if needed.